Canonical Allele Identifier: CA875200427

Gene: TSPAN7

Linked Data

• dbSNP Id: rs1431634438
• gnomAD v3: X-38675974-TCTTA-T
• gnomAD v4: X-38675974-TCTTA-T
• MyVariant Identifiers: chrX:g.38535229_38535232del (hg19) ; chrX:g.38675975_38675978del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675978_38675981del , CM000685.2:g.38675978_38675981del	GRCh38
NC_000023.10:g.38535232_38535235del , CM000685.1:g.38535232_38535235del	GRCh37
NC_000023.9:g.38420176_38420179del	NCBI36
NG_009160.1:g.119502_119505del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+118_597+121del MANE Select	ENSP00000367743.2:n.597+118_597+121del
ENST00000286824.6:c.648+118_648+121del	ENSP00000286824.6:n.648+118_648+121del
ENST00000378482.6:c.597+118_597+121del	ENSP00000367743.2:n.597+118_597+121del
ENST00000419600.3:n.541+118_541+121del
ENST00000465127.1:c.687+118_687+121del	ENSP00000417050.1:n.687+118_687+121del
ENST00000471410.5:c.*623+118_*623+121del	ENSP00000419290.1:n.*623+118_*623+121del
ENST00000475216.5:c.*590+118_*590+121del	ENSP00000418586.1:n.*590+118_*590+121del
NM_004615.3:c.597+118_597+121del	NP_004606.2:n.597+118_597+121del
NM_004615.4:c.597+118_597+121del MANE Select	NP_004606.2:n.597+118_597+121del